US9095560B2ExpiredUtilityA1
Method of enhancing transdermal absorption using a composition comprising POE octyl dodecyl ether and squalane
Est. expiryApr 28, 2025(expired)· nominal 20-yr term from priority
A61P 3/02A61P 3/10A61K 47/12A61K 9/06A61P 17/02A61K 9/1274A61K 47/44A61K 31/203A61K 31/23A61K 9/0014A61K 9/10
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Claims
Abstract
An object of the present invention is to provide a transdermal absorption enhancer by which various active ingredients are transdermally absorbed. In accordance with a transdermal absorption enhancer of the present invention which effective ingredient is lyotropic liquid crystal which has been utilized as a basic material for pharmaceutical preparations for external application and for cosmetics, transdermal absorption of a macromolecular substance and a water-soluble substance was able to be improved.
Claims
exact text as granted — not AI-modifiedThe invention claimed is:
1. A method of transdermally administering an active ingredient, comprising:
applying a lyotropic liquid crystal compounded with the active ingredient to a skin surface of a person in need of transdermal administration of the active ingredient,
wherein said lyotropic liquid crystal contains 15.026% by weight to 28% by weight of a surfactant and 5% by weight to 80% by weight of water,
wherein said active ingredient is a macromolecular substance having a molecular weight of not less than 1,000 daltons,
wherein said surfactant is polyoxyethylene octyl dodecyl ether,
wherein said lyotropic liquid crystal further contains 16.819% by weight to 25% by weight of squalane,
wherein said lyotropic liquid crystal further contains 1% by weight to 55% by weight of glycerol.
2. The method of claim 1 , wherein said lyotropic liquid crystal further contains 0.01% by weight to 10% by weight of an auxiliary surfactant.
3. The method of claim 2 , wherein said auxiliary surfactant is cholesterol.
4. The method of claim 1 , wherein said active ingredient is at least one member selected from the group consisting of organic compound, peptide, protein, oligonucleotide, DNA and RNA.
5. The method of claim 1 , wherein said macromolecular substance is a water-soluble substance.
6. The method of claim 1 , wherein said active ingredient is included in the inside of fine particles of inorganic acid salt with divalent metal.
7. The method of claim 1 , wherein said active ingredient is compounded in an amount of 0.01% by weight to 50% by weight to the lyotropic liquid crystal.
8. The method of claim 1 , wherein the ratio of each component in the lyotropic liquid crystal is as follows:
polyoxyethylene octyl dodecyl ether: 28% by weight,
squalane: 25% by weight,
water: 16% by weight, and
glycerol: 31% by weight.
9. The method of claim 1 , wherein the ratio of each component in the lyotropic liquid crystal is as follows:
polyoxyethylene octyl dodecyl ether: 15.026% by weight,
squalane: 16.819% by weight,
water: 15.860% by weight, and
glycerol: 38.897% by weight.
10. The method of claim 1 , wherein said lyotropic liquid crystal contains 10% by weight to 60% by weight of water.
11. The method of claim 1 , wherein said lyotropic liquid crystal contains 13% by weight to 50% by weight of water.Cited by (0)
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